Panax Ginseng Protects Against Doxorubicin-Induced Testicular Injury in Male Rats by Modulating NF-κB/COX-2 and AR Pathways
Özet
Panax ginseng (PG) is a medicinal plant used for many years to treat many diseases. The current study aimed to investigate the possible prophylactic and therapeutic effects of PG extract on doxorubicin (DOX)-induced testicular toxicity in rats. 32 adult male Sprague–Dawley rats (200–250 g) were used in the experiment. The experimental groups were designed as control (normal saline, intraperitoneal), DOX (18 mg/kg, intraperitoneal), PG (200 mg/kg, gavage), and PG + DOX (200 mg/kg, gavage). After treatment, serum levels of testosterone, interleukin-1β (IL-1β), glutathione (GSH), luteinizing hormone (LH), superoxide dismutase (SOD), lactate dehydrogenase (LDH), catalase (CAT), follicle stimulating hormone (FSH), tumor necrosis factor-α (TNF-α), and malondialdehyde (MDA) were measured. Then, gene expression, histopathological, and immunohistochemical analyses were performed on testicular tissues. Compared to DOX, treatment with PG + DOX showed a significant improvement in serum levels of FSH, testosterone, LH, TNF-α, IL-1β, MDA, SOD, LDH, GSH, and CAT. It was also observed that PG + DOX decreased nuclear factor-κB and cyclooxygenase-2 expression levels, increased androgen receptor expression, restored testicular histopathological structure, and significantly improved spermatogenesis. The results of the present study showed that PG may have an ameliorative effect against DOX-induced male reproductive toxicity, as DOX causes male reproductive toxicity. It can be concluded that PG is one of the effects that protect against DOX-induced testicular toxicity in rats by reducing lipid peroxidation and activating the antioxidant system. In light of this information, PG may be a useful agent to prevent the testicular toxicity observed in men receiving DOX treatment. © The Author(s) 2025.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Yeni, Yesim | |
| dc.contributor.author | Cicek, Betul | |
| dc.contributor.author | Hacimuftuoglu, Ahmet | |
| dc.contributor.author | Ozkaraca, Mustafa | |
| dc.contributor.author | Mokhtare, Behzad | |
| dc.date.accessioned | 2026-10-18T20:26:02.029084615Z | |
| dc.date.available | 2026-10-18T20:26:02.029084615Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Panax ginseng (PG) is a medicinal plant used for many years to treat many diseases. The current study aimed to investigate the possible prophylactic and therapeutic effects of PG extract on doxorubicin (DOX)-induced testicular toxicity in rats. 32 adult male Sprague–Dawley rats (200–250 g) were used in the experiment. The experimental groups were designed as control (normal saline, intraperitoneal), DOX (18 mg/kg, intraperitoneal), PG (200 mg/kg, gavage), and PG + DOX (200 mg/kg, gavage). After treatment, serum levels of testosterone, interleukin-1β (IL-1β), glutathione (GSH), luteinizing hormone (LH), superoxide dismutase (SOD), lactate dehydrogenase (LDH), catalase (CAT), follicle stimulating hormone (FSH), tumor necrosis factor-α (TNF-α), and malondialdehyde (MDA) were measured. Then, gene expression, histopathological, and immunohistochemical analyses were performed on testicular tissues. Compared to DOX, treatment with PG + DOX showed a significant improvement in serum levels of FSH, testosterone, LH, TNF-α, IL-1β, MDA, SOD, LDH, GSH, and CAT. It was also observed that PG + DOX decreased nuclear factor-κB and cyclooxygenase-2 expression levels, increased androgen receptor expression, restored testicular histopathological structure, and significantly improved spermatogenesis. The results of the present study showed that PG may have an ameliorative effect against DOX-induced male reproductive toxicity, as DOX causes male reproductive toxicity. It can be concluded that PG is one of the effects that protect against DOX-induced testicular toxicity in rats by reducing lipid peroxidation and activating the antioxidant system. In light of this information, PG may be a useful agent to prevent the testicular toxicity observed in men receiving DOX treatment. © The Author(s) 2025. | |
| dc.description.sponsorship | Open access funding provided by the Scientific and Technological Research Council of T\u00FCrkiye (T\u00DCB\u0130TAK). The authors did not receive any financial support. | |
| dc.identifier.doi | 10.1007/s12035-025-05116-9 | |
| dc.identifier.eissn | 1559-1182 | |
| dc.identifier.endpage | 12850 | |
| dc.identifier.issn | 0893-7648 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pmcid | PMC12433337 | |
| dc.identifier.pmid | 40451973 | |
| dc.identifier.scopus | 2-s2.0-105006903736 | |
| dc.identifier.startpage | 12839 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/10921 | |
| dc.identifier.volume | 62 | |
| dc.identifier.wos | WOS:001499384700001 | |
| dc.language.iso | en | |
| dc.publisher | Springer | |
| dc.relation.ispartof | Molecular Neurobiology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Doxorubicin | |
| dc.subject | Male Fertility | |
| dc.subject | Oxidative Stress | |
| dc.subject | Panax Ginseng | |
| dc.subject | Real-Time PCR | |
| dc.subject | Animals | |
| dc.subject | Cyclooxygenase 2 | |
| dc.subject | Male | |
| dc.subject | Malondialdehyde | |
| dc.subject | NF-kappa B | |
| dc.subject | Panax | |
| dc.subject | Plant Extracts | |
| dc.subject | Protective Agents | |
| dc.subject | Rats | |
| dc.subject | Rats, Sprague-Dawley | |
| dc.subject | Receptors, Androgen | |
| dc.subject | Signal Transduction | |
| dc.subject | Testis | |
| dc.subject | Testosterone | |
| dc.subject | antioxidant | |
| dc.subject | catalase | |
| dc.subject | follitropin | |
| dc.subject | ginseng extract | |
| dc.subject | glutathione | |
| dc.subject | interleukin 1beta | |
| dc.subject | lactate dehydrogenase | |
| dc.subject | luteinizing hormone | |
| dc.subject | malonaldehyde | |
| dc.subject | superoxide dismutase | |
| dc.subject | thiopental | |
| dc.title | Panax Ginseng Protects Against Doxorubicin-Induced Testicular Injury in Male Rats by Modulating NF-κB/COX-2 and AR Pathways | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 3 | |
| rdl.citation.wos | 4 | |
| rdl.department | Faculty of Medicine, Department of Physiology, Erzincan Binali Yildirim University, Erzincan, Turkey. | |
| rdl.oa.status | gold | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
